3-KETO HMG-CoA reductase inhibitors

ABSTRACT

Processes and intermediates are disclosed for the formation of compounds of formula (I) and (II): ##STR1##

This is a continuation-in-part of U.S. patent application Ser. No.363,736, filed June 9, 1989

BACKGROUND OF THE INVENTION

Hypercholesterolemia is known to be one of the prime risk factors forischemic cardiovascular disease, such as arteriosclerosis. Bile acidsequestrants have been used to treat this condition; they seem to bemoderately effective but they must be consumed in large quantities, i.e.several grams at a time and they are not very palatable.

MEVACOR™ (lovastatin), now commercially available, is one of a group ofvery active antihypercholesterolemic agents that function by limitingcholesterol biosynthesis by inhibiting the enzyme, HMG-CoA reductase. Inaddition to the natural fermentation products, mevastatin andlovastatin, there are a variety of analogs thereof, produced bymicrobial, enzymatic and synthetic techniques.

The naturally occurring compounds and their analogs have the followinggeneral structural formulae: ##STR2## wherein: R¹ is hydrogen, C₁₋₅alkyl or C₁₋₅ alkyl substituted with a member of the group consisting ofphenyl, dimethylamino, or acetylamino; and

R* is ##STR3## wherein Q is ##STR4## R³ is H or OH or Q is ##STR5## M is--CHR⁴, R⁴ is hydrogen or hydroxy; X is CR⁵ R⁶, O, S, or NH; R⁵ and R⁶are H, OH, or OR⁷ where R⁷ represents a phosphoryl or acyl moiety;

R² is hydrogen or methyl; and a, b, c, and d represent single bonds, oneof a, b, c or d represents a double bond, or both a and c or both b andd represent double bonds provided that when a is a double bond, Q is##STR6## and when d is a double bond, M is ##STR7## and provided thatwhen R⁵ or R⁶ is OH or OR⁷ or X is O, S, or NH, a, b, and c are singlebonds.

U.S. Pat. No. 4,517,373 discloses hydroxy containing compoundsrepresented by the above general formula wherein R* is ##STR8##

U.S. Pat. Nos. 4,537,859 and 4,448,979 also disclose hydroxy-containingcompounds represented by the above general formula wherein R* is##STR9##

These compounds are prepared by the action of certain microorganisms onthe corresponding non-hydroxylated substrates. One such organismdescribed in U.S. Pat. No. 4,537,859 is of the genus Nocardia.

U.K. Patent No. 2,075,013 discloses hydroxy containing compoundsrepresented by the above general formula wherein R* is: ##STR10##wherein R¹ is H or Me, and R² is H or acyl.

U.S. patent application Ser. No. 254,525 filed Oct. 6, 1988 discloses6-substituted compounds of the above general formula wherein R* is:##STR11## wherein R is CH₂ OH, ##STR12## CO₂ R⁷ or ##STR13## and R¹, R⁴,R⁷, R⁸ and R⁹ are broadly defined organic moieties.

U.S. Pat. Nos. 4,604,472 and 4,733,003 disclose compounds of the aboveformula wherein R* is: ##STR14## wherein X represents a hydrogen atom ora 2-methylbutyryl group, Y represents a hydrogen atom or a methyl groupand R¹ and R² are the same or different and each represents an oxygenatom or a group of formula =N-OR³ where R³ is a hydrogen or alkylmoiety.

DETAILED DESCRIPTION OF THE INVENTION

This invention relates to HMG-CoA reductase inhibitors of structuralformulae (I) and (II), and to processes and intermediates for formingcompounds of formula (I): ##STR15## wherein: R₁ is selected from:

(1) C₁₋₁₀ alkyl;

(2) substituted C₁₋₁₀ alkyl in which one or more substituent(s) isselected from

(a) halogen,

(b) hydroxy,

(c) C₁₋₁₀ alkoxy,

(d) C₁₋₅ alkoxycarbonyl,

(e) C₁₋₅ acyloxy,

(f) C₃₋₈ cycloalkyl,

(g) phenyl,

(h) substituted phenyl in which the substituents are X and Y,

(i) C₁₋₁₀ alkylS(O)_(n) in which n is 0 to 2,

(j) C₃₋₈ cycloalkylS(O)_(n),

(k) phenylS(O)_(n),

(l) substituted phenylS(O)_(n) in which the substituents are X and Y,and

(m) oxo;

(3) C₁₋₁₀ alkoxy;

(4) C₂₋₁₀ alkenyl;

(5) C₃₋₈ cycloalkyl;

(6) substituted C₃₋₈ cycloalkyl in which one substituent is selectedfrom

(a) C₁₋₁₀ alkyl

(b) substituted C₁₋₁₀ alkyl in which the substituent is selected from

(i) halogen,

(ii) hydroxy,

(iii) C₁₋₁₀ alkoxy,

(iv) C₁₋₅ alkoxycarbonyl,

(v) C₁₋₅ acyloxy,

(vi) phenyl,

(vii) substituted phenyl in which the substituents are X and Y

(viii) C₁₋₁₀ alkylS(O)_(n),

(ix) C₃₋₈ cycloalkylS(O)_(n),

(x) phenylS(O)_(n),

(xi) substituted phenylS(O)_(n) in which the substituents are X and Y,and

(xii) oxo,

(c) C₁₋₁₀ alkylS(O)_(n),

(d) C₃₋₈ cycloalkylS(O)_(n),

(e) phenylS(O)_(n),

(f) substituted phenylS(O)_(n) in which the substituents are X and Y,

(g) halogen,

(h) hydroxy,

(i) C₁₋₁₀ alkoxy,

(j) C₁₋₅ alkoxycarbonyl,

(k) C₁₋₅ acyloxy,

(l) phenyl, and

(m) substituted phenyl in which the substituents are X and Y;

(7) phenyl;

(8) substituted phenyl in which the substituents are X and Y;

(9) amino;

(10) C₁₋₅ alkylamino;

(11) di(C₁₋₅ alkyl)amino;

(12) phenylamino;

(13) substituted phenylamino in which the substituents are X and Y;

(14) phenyl C₁₋₁₀ alkylamino;

(15) substituted phenyl C₁₋₁₀ alkylamino in which the substituents are Xand Y;

(16) a member selected from

(a) piperidinyl,

(b) pyrrolidinyl,

(c) piperazinyl,

(d) morpholinyl, and

(e) thiomorpholinyl; and

(17) R₃ S in which R₃ is selected from

(a) C₁₋₁₀ alkyl,

(b) phenyl, and

(c) substituted phenyl in which the substituents are X and Y;

R₂ is H, CH₃, or CH₂ OH;

X and Y are independently selected from:

(a) OH,

(b) halogen,

(c) trifluoromethyl,

(d) C₁₋₃ alkoxy,

(e) C₁₋₃ alkylcarbonyloxy,

(f) phenylcarbonyloxy,

(g) C₁₋₃ alkoxycarbonyl,

(h) phenyloxycarbonyl,

(i) hydrogen;

(j) C₁₋₅ alkyl;

Z is selected from

(1) hydrogen;

(2) C₁₋₅ alkyl;

(3) substituted C₁₋₅ alkyl in which the substituent is selected from

(a) phenyl,

(b) dimethylamino, and

(c) acetylamino, and

(4) 2,3 hydroxypropyl;

halogen is Cl or F;

a is a single bond or a double bond;

and pharmaceutically acceptable salts of the compound (II) in which Z ishydrogen.

Except where specifically defined to the contrary, the terms "alkyl","alkenyl", "acyl" "aryloxy" and "alkoxy" include both the straight-chainand branched-chain species of the term.

One embodiment of this invention is the class of compounds of formulae(I) and (II) and the processes and intermediates for forming this classof compounds of formula (I) wherein:

R₁ is selected from:

(1) C₁₋₁₀ alkyl;

(2) substituted C₁₋₁₀ alkyl in which one or more substituent(s) isselected from

(a) halogen,

(b) hydroxy,

(c) C₁₋₁₀ alkoxy,

(d) C₁₋₅ alkoxycarbonyl,

(e) C₁₋₅ acyloxy,

(f) C₃₋₈ cycloalkyl,

(g) phenyl,

(h) substituted phenyl in which the substituents are X and Y, and

(i) oxo;

(3) C₃₋₈ cycloalkyl;

(4) substituted C₃₋₈ cycloalkyl in which one substituent is selectedfrom

(a) C₁₋₁₀ alkyl,

(b) substituted C₁₋₁₀ alkyl in which the substituent is selected from

(i) halogen,

(ii) hydroxy,

(iii) C₁₋₁₀ alkoxy,

(iv) C₁₋₅ acyloxy,

(v) C₁₋₅ alkoxycarbonyl,

(vi) phenyl,

(vii) substituted phenyl in which the substituents are X and Y, and

(viii) oxo,

(c) halogen,

(d) hydroxy,

(e) C₁₋₁₀ alkoxy,

(f) C₁₋₅ alkoxycarbonyl,

(g) C₁₋₅ acyloxy,

(h) phenyl,

(i) substituted phenyl in which the substituents are X and Y;

(5) phenylamino;

(6) substituted phenylamino in which the substituents are X and Y;

(7) phenylC₁₋₁₀ alkylamino; and

(8) substituted phenyl C₁₋₁₀ alkylamino in which the substituents are Xand Y;

X and Y are independently selected from:

(a) OH,

(b) F,

(c) trifluoromethyl,

(d) C₁₋₃ alkoxy,

(e) hydrogen,

(f) C₁₋₅ alkyl.

In one subclass are the compounds of formulae (I) and (II) and theprocesses and intermediates for forming compounds of formula (I) whereinR₁ is C₁₋₁₀ alkyl.

Illustrating this subclass are those compounds of formulae (I) and (II)and the processes and intermediates wherein:

R₁ is 2-butyl or 2-methyl-2-butyl; and

R₂ is H or CH₃.

Exemplifying this subclass are the following compounds:

(1)6(R)-[2-[8(S)-(2-methylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(2)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(3)6(R)-[2-[8(S)-(2-methylbutyryloxy)-2(S)-methyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(4)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S)-methyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(5)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-3-oxo-1,2,3,5,6,7,8,8a(R)-octahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(6)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S)-methyl-3-oxo-1,2,3,5,6,7,8,8a(R)-octahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one.

(7)6(R)-[2-[8(S)-(2-methylbutyryloxy)-2(S),6(R)-dimethyl-3-oxo-1,2,3,5,6,7,8,8a(R)-octahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one;

(8)6(R)-[2-[8(S)-(2-methylbutyryloxy)-2(S)-methyl-3-oxo-1,2,3,5,6,7,8,8a(R)-octahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one.

The compounds of formulae (I) and (II) wherein R₂ is methyl and a is adouble bond, may be prepared from lovastatin or simvastatin or itsanalogs having a 6-methyl group by one of the following microbiologicalprocedures:

(a) adding the substrate to a growing culture of Nocardia autotrophicafor a suitable incubation period followed by isolation, andderivatization if desired;

(b) collecting a culture of the bioconverting microorganism andcontacting the collected cells with the substrate; or

(c) preparing a cell-free, enzyme-containing extract from the cells ofthe bioconverting microorganism and contacting this extract with thesubstrate.

Cultivation of the bioconverting microorganism of the genus Nocardia canbe carried out by conventional means in a conventional culture mediumcontaining nutrients well known for use with such microorganisms. Thus,as is well known, such culture media contain sources of assimilablecarbon and of assimilable nitrogen and often inorganic salts. Examplesof sources of assimilable carbon include glucose, sucrose, starch,glycerin, millet jelly, molasses and soybean oil. Examples of sources ofassimilable nitrogen include soybean solids (including soybean meal andsoybean flour), wheat germ, meat extracts, peptone, corn steep liquor,dried yeast and ammonium salts, such as ammonium sulphate. If required,inorganic salts, such as sodium chloride, potassium chloride, calciumcarbonate or phosphates, may also be included. Also, if desired, otheradditives capable of promoting the production of hydroxylation enzymesmay be employed in appropriate combinations. The particular cultivationtechnique is not critical to the process of the invention and anytechniques conventionally used for the cultivation of microorganisms mayequally be employed with the present invention. In general, of course,the techniques employed will be chosen having regard to industrialefficiency. Thus, liquid culture is generally preferred and the deepculture method is most convenient from the industrial point of view.

Cultivation will normally be carried out under aerobic conditions and ata temperature within the range from 20° to 37° C., more preferably from26° to 28° C.

Method (a) is carried out by adding the substrate to the culture mediumin the course of cultivation. The precise point during the cultivationat which the starting compound is added will vary depending upon thecultivation equipment, composition of the medium, temperature of theculture medium and other factors, but it is preferably at the time whenthe hydroxylation capacity of the microorganism begins to increase andthis is usually 1 or 2 days after beginning cultivation of themicroorganism. The amount of the substrate added is preferably from 0.01to 5.0% by weight of the medium, more preferably from 0.05 to 0.5%,e.g., from 0.05 to 0.1% by weight. After addition of the substrate,cultivation is continued aerobically, normally at a temperature withinthe ranges proposed above. Cultivation is normally continued for aperiod of from 1 to 2 days after addition of the substrate.

In method (b), cultivation of the microorganism is first carried outunder conditions such as to achieve its maximum hydroxylation capacity;this capacity usually reaches a maximum between 4 and 5 days afterbeginning the cultivation, although this period is variable, dependingupon the nature and temperature of the medium, the species ofmicroorganism and other factors. The hydroxylation capacity of theculture can be monitored by taking samples of the culture at suitableintervals, determining the hydroxylation capacity of the samples bycontacting them with a substrate under standard conditions anddetermining the quantity of product obtained and plotting this capacityagainst time as a graph. When the hydroxylation capacity has reached itsmaximum point, cultivation is stopped and the microbial cells arecollected. This may be achieved by subjecting the culture to centrifugalseparation, filtration or similar known separation methods. The wholecells of the cultivating microorganism thus collected, preferably, arethen washed with a suitable washing liquid, such as physiological salineor an appropriate buffer solution.

Contact of the collected cells of the microorganism of the genusNocardia with the substrate is generally effected in an aqueous medium,for example in a phosphate buffer solution at a pH value of from 5 to 9.The reaction temperature is preferably within the range from 20° to 45°C., more preferably from 25° to 30° C. The concentration of thesubstrate in the reaction medium is preferably within the range from0.01 to 5.0% by weight. The time allowed for the reaction is preferablyfrom 1 to 5 days, although this may vary depending upon theconcentration of the substrate in the reaction mixture, the reactiontemperature, the hydroxylation capacity of the microorganism (which may,of course, vary from species to species and will also, as explainedabove, depend upon the cultivation time) and other factors.

The cell-free, enzyme-containing extract employed in method (c) may beobtained by breaking down the whole cells of the microorganism obtainedas described in relation to method (b) by physical or chemical means,for example by grinding or ultrasonic treatment to provide adisintegrated cellular mass or by treatment with a surface active agentor an enzyme to produce a cellular solution. The resulting cell-freeextract is then contacted with the substrate under the same conditionsas are described above in relation to method (b).

The microorganism useful in the novel process of this invention is ofthe genus Nocardia. Of particular importance are the known strains ofmicroorganism, Nocardia autotrophica, subspecies canberrica, ATCC 35203of the culture MA-6181 and subspecies amethystina ATCC 35204 of theculture MA-6180 of the culture collection of Merck & Co., Inc., Rahway,N.J. A sample of the culture designated ATCC 35203 and ATCC 35204 isavailable in the permanent culture collection of the American TypeCulture Collection at 12301 Parklawn Drive, Rockville, Md. 20852.

After completion of the conversion reaction by any of the above methods,the desired compound can be directly isolated, separated or purified byconventional means. For example, separation and purification can beeffected by filtering the reaction mixture, extracting the resultingfiltrate with a water-immiscible organic solvent (such as ethylacetate), distilling the solvent from the extract, subjecting theresulting crude compound to column chromatography, (for example onsilica gel or alumina) and eluting the column with an appropriateeluent, especially in an HPLC apparatus.

Where the acyl moiety of formulae (I) or (II) is other than2-methylbutyryl or 2,2-dimethylbutyryl, the acyl moiety of lovastatinmay be hydrolyzed and the hydroxyl group reesterified with anappropriate alkanoyl halide following the procedure in U.S. Pat. No.4,444,784. The alkanoyl halide can be formed by standard transformationssuch as substitution with an alkyl halide or other appropriateelectrophile at an acidic C-H site on an available starting material.See for example U.S. Pat. No. 4,766,145 and allowed pending U.S. patentapplications Ser. Nos. 205,406 and 205,407 filed June 10, 1988.

Starting material (1) wherein R₂ is CH₂ OH may be prepared following theprocedures in copending U.S. patent application Ser. No. 254,525 filedOct. 6, 1988. The hydroxy group may be protected with a suitable alcoholprotecting group employing a trialkylsilyl chloride or aalkyldiarylsilyl chloride or dihydropyran.

The compounds of formulae (I) and (II) may also be prepared followingthe synthetic methodology in Scheme 1. ##STR16##

Starting material (1) is treated with a reagent suitable for protectingthe alcohol group at the lactone 4-position. Examples of suitablereagents are trialkylsilyl chlorides, alkyldiarylsilyl chlorides anddihydropyran.

The diene (2) is treated with a halogenating agent such as phenylselenylchloride or bromide or phenylsulfinyl chloride, preferably phenylselenylchloride, in an approximately equimolar ratio in an inert solvent atabout -80° C., for approximately 20 minutes; illustrative of such inertsolvents are methylene chloride, ether and the like. After a standardworkup the product residue is dissolved in an ethereal solvent, chilledto about 0° C. and oxidized with an agent such as 30% hydrogen peroxideor a peroxy acid such as peroxybenzoic acid to yield a halohydrin analog(3).

Intermediate (3) is treated with a halide reducing agent such as atrialkyltin hydride or a triaryltin hydride, preferably tri-n-butyltinhydride and a radical initiator such as azobisisobutyronitrile (AIBN) inan inert solvent such as benzene at a temperature between 70° C. and100° C. preferably about 90° C. for 0.5 to 5 hours preferably 2 hours,to yield compound (4).

Compound (4) is treated with pyridinium chlorochromate (PCC) on aluminumoxide in toluene to yield the enone (5). Compound (5) is contacted witha trialkylsilyl or alkyldiarylsilyl trifluoromethanesulfonate such astrimethylsilyl trifluoromethanesulfonate and an amine to yield thetrialkylsilyl ether diene (6). Compound (6) is treated with palladiumacetate in acetonitrile to form dienone (7). Hydroxyl protecting groupsare removed by treatment with tetrabutyl ammonium fluoride and aceticacid in tetrahydrofuran or aqueous hydrofluoric acid in acetonitrile toyield product (I). Silyl ether cleavage reagents other than fluoride oracid cleavage could be employed depending on the particular silyl etherprotecting agent, such cleavage reagents are listed in the textProtective Groups in Organic Synthesis, T. W. Greene, John Wiley & Sons,(1981).

Enone (5) can be converted to compounds of formula (I) wherein a is asingle bond by treatment with tetrabutyl ammonium fluoride in aceticacid.

Alternatively the compounds of formulae (I) can be prepared followingthe synthetic outline of Scheme 2. ##STR17##

Diene starting material (1) is converted to epoxides (8) and (9) bytreatment with m-chloroperoxybenzoic acid at about 0° C. The mixture ofepoxides is then contacted with tris(dibenzylideneacetone)-dipalladium(0) and triisopropoxy phosphine toyield the mixture of hydroxy dienes (10) and (11). This mixture is thenoxidized with PCC attenuated with 3,5 dimethylpyrazole to yield 5-onecompound (12) and product (I).

Enone (5) of Scheme 1 can also be formed from hydroxyl protected epoxide(9) or the mixture of epoxides (8) and (9) as shown below: ##STR18##

Compound (5) can then be employed in Scheme 1 to form product (I).

Alternatively, the compounds of formula (I) may be prepared in amodified sequence of Scheme 1 as shown in Scheme 3 below: ##STR19##

Halohydrin (3) is treated with PCC on Al₂ O₃ in toluene to yield theenone (13). Compound (13) is deprotected to yield compound (14)employing a silyl ether hydrolysis reagent such as those described inthe test by T. W. Greene, Protective Groups in Organic Synthesis, J.Wiley (1981). The preferred hydrolysis reagents are HF/CH₃ CN or (n-Bu)₄N⁺ F⁻. Compound (14) is dehydrohalogenated using:

(a) NaI in a low boiling ketone, such as 2-butanone, or acetone or2-pentanone or 3-pentanone, preferably 2-butanone; or

(b) LiBr·Li₂ CO₃ in DMF at about 150° C. for about 10 hours; or

(c) Collidine at about 170° C. for about 4 hours;

The preferred dehydrohalogenating agent is NaI/2-butanone.

Where the reaction conditions of the above noted chemicaltransformations would be deleterious to the substituents in the8-acyloxy moiety, the acetoxy group can be employed as a protectinggroup which after the elaboration elsewhere in the molecule can beremoved by hydrolysis to give the 8-hydroxy derivative which then can beacylated according to the general procedures described in U.S. Pat. No.4,661,483.

Where the product formed by the above described synthetic pathways isnot the desired form of that compound, then that product may besubjected to one or more further reactions such as hydrolysis,disilylation, salification, esterification, acylation, ammonolysis orlactonization by conventional methods.

Preferred metal salts are salts with alkali metals, such as sodium orpotassium, salts with alkaline earth metals, such as calcium, or saltswith other metals such as magnesium, aluminum, iron, zinc, copper,nickel or cobalt, of which the alkali metal, alkaline earth metal,magnesium and aluminum salts are preferred, the sodium, calcium andaluminum salts being most preferred.

Preferred amino acids to form amino acid salts are basic amino acids,such as arginine, lysine, α,β-diaiminobutyric acid or ornithine.

Preferred amines to form amine salts include t-octylamine,dibenzylamine, ethylenediamine, morpholine, andtris(hydroxymethyl)aminomethane. Also preferred is ammonia to form theammonium salt.

Esters are preferably the alkyl esters, such as the methyl, ethyl,propyl, isopropyl, butyl, isobutyl, or pentyl esters, of which themethyl ester is preferred. However, other esters such as phenyl-C₁₋₅alkyl, dimethylamino-C₁₋₅ alkyl, or acetylamino-C₁₋₅ alkyl may beemployed if desired.

Metal salts of the carboxylic acids of formula (II) may be obtained bycontacting a hydroxide, carbonate or similar solvent with the carboxylicacid of formula (II). The aqueous solvent employed is preferably water,or it may be a mixture of water with an organic solvent, preferably analcohol (such as methanol or ethanol), a ketone (such as acetone), analiphatic hydrocarbon (such as hexane) or an ester (such as ethylacetate). It is preferred to use a mixture of a hydrophilic organicsolvent with water. Such reactions are normally conducted at ambienttemperature but they may, if desired, be conducted with heating orcooling.

Amine salts of the carboxylic acids of formula (II) may be obtained bycontacting an amine in an aqueous solvent with the carboxylic acid offormula (II). Suitable aqueous solvents include water and mixtures ofwater with alcohols (such as methanol or ethanol), ethers (such asdiethyl ether and tetrahydrofuran), nitriles (such as acetonitrile) orketones (such as acetone); it is preferred to use aqueous acetone as thesolvent for this reaction. The reaction is preferably carried out at atemperature of ambient or below, more preferably a temperature of from5° to 10° C. The reaction immediately goes to completion. Alternatively,a metal salt of the carboxylic acid of formula (II) (which may have beenobtained as described above) can be dissolved in an aqueous solvent,after which a mineral acid salt (for example the hydrochloride) of thedesired amine is added, employing the same reaction conditions as whenthe amine itself is reacted with the carboxylic acid of formula (II) andthe desired product is then obtained by metathesis.

Amino acid salts of the carboxylic acids of formula (II) may be obtainedby contacting an amino acid in aqueous solution with the carboxylic acidof formula (II). Suitable aqueous solvents include water and mixtures ofwater with alcohols (such as methanol or ethanol) or ethers (such astetrahydrofuran).

Esters, preferably alkyl esters, of the carboxylic acids of formula (II)may be obtained by contacting the carboxylic acid of formula (II) withan appropriate alcohol, preferably in the presence of an acid catalyst,for example a mineral acid (such as hydrochloric acid or sulphuricacid), a Lewis acid (for example boron trifluoride) or an acidic ionexchange resin. The solvent employed for this reaction is not critical,provided that it does not adversely affect the reaction; suitablesolvents include the alcohol itself, benzene, chloroform, ethers and thelike. Alternatively, the desired product may be obtained by contactingthe carboxylic acid of formula (II) with a diazoalkane, in which thealkane moiety may be substituted or unsubstituted. This reaction isusually effected by contacting the acid with an ethereal solution of thediazoalkane. As a further alternative, the ester may be obtained bycontacting a metal salt of the carboxylic acid of formula (II) with ahalide, preferably an alkyl halide, in a suitable solvent; preferredsolvents include dimethylformamide, tetrahydrofuran, dimethylsulfoxideand acetone. Finally, esters may also be obtained from the lactone offormula (I) by reaction with an appropriate alkoxide in an absolutealkanol. All of the reactions for producing esters are preferablyeffected at about ambient temperature, but, if required by the nature ofthe reaction system, the reactions may be conducted with heating orcooling.

Lactones of the carboxylic acids of formula (I) may be obtained bylactonizing the carboxylic acids of formula (II) under ordinaryconditions known to one skilled in the art.

The intrinsic HMG-CoA reductase inhibition activity of the claimedcompounds is measured in the in vitro protocol published in J. Med.Chem., 28, p. 347-358 (1985).

Included within the scope of this invention are the intermediates andprocesses for forming compounds of formula (I).

The compounds of this invention are useful as antihypercholesterolemicagents for the treatment of arteriosclerosis, hyperlipidemia, familialhypercholesterolemia and the like diseases in humans. They may beadministered orally or parenterally in the form of a capsule, a tablet,an injectable preparation or the like. It is usually desirable to usethe oral route. Doses may be varied, depending on the age, severity,body weight and other conditions of human patients but daily dosage foradults is within a range of from about 2 mg to 2000 mg (preferably 10 to100 mg) which may be given in two to four divided doses. Higher dosesmay be favorably employed as required.

The compounds of this invention may also be coadministered withpharmaceutically acceptable nontoxic cationic polymers capable ofbinding bile acids in a non-reabsorbable form in the gastro-intestinaltract. Examples of such polymers include cholestyramine, colestipol andpoly[methyl-(3-trimethylaminopropyl)imino-trimethylene dihalide]. Therelative amounts of the compounds of this invention and these polymersis between 1:100 and 1:15,000.

Included within the scope of this invention is the method of treatingarteriosclerosis, familial hypercholesterolemia or hyperlipidemia whichcomprises administering to a subject in need of such treatment anontoxic, therapeutically-effective amount of the compounds of formulae(I) or (II) or pharmaceutical compositions thereof.

The following examples illustrate the preparation of the compounds ofthe formulae (I) and (II) and their incorporation into pharmaceuticalcompositions and as such are not to be considered as limiting theinvention set forth in the claims appended hereto.

EXAMPLE 1 Preparation of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

Utilizing the general procedure for the bioconversion of sodium salt of7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid as described in co-pending U.S. patent application Ser. No.254,525, filed Oct. 6, 1988 the above titled compound was isolated as aminor product.

The following media are utilized in the bioconversion reactionsdescribed below:

    ______________________________________                   Grams per liter    Medium A       distilled water    ______________________________________    Yeast extract  4.0    Malt extract   10.0    Nutrient broth 4.0    Dextrose       4.0    pH 7.4    ______________________________________

Medium sterilized for 20 min. at 121° C.

    ______________________________________                    Grams per liter    Medium B        distilled water    ______________________________________    Dextrose        10.0    Polypeptone     2.0    Meat extract    1.0    Corn steep liquor                    3.0    pH 7.0    ______________________________________

Medium sterilized for 20 min. at 121° C.

I. Culture Conditions and Bioconversion

A lyophilized tube of Nocardia autotrophica subsp. canberrica ATCC 35204(MA-6180) was used to inoculate 18×175 agar slants (Medium A) which wereincubated at 27° C. for 7 days. The slant culture was washed with 5 mlof sterile medium B and transferred to a 250 ml flask containing 50 mlof sterile medium B. This first stage seed was grown at 27° C. on a 220rpm shaker and, after 24 hours, 2 ml was transferred to another flask ofsterile medium B.

Grown under the above conditions, the second seed was used to start thebioconversion culture: 20 ml of the seed culture was placed in 400 ml ofsterile medium B in a 2 L flask. After the culture had grown for 24hours, 80 mg of the sodium salt of7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid was added to each flask. The incubation was continued for 28 hoursor until no7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid could be detected by HPLC. The whole broth was clarified bycentrifugation followed by filtration through Whatman No. 2 filterpaper.

II. HPLC Methods

Aliquots of whole broth could be analyzed for7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid derivatives by HPLC. Filtered broth could be injected directly (10to 20 μl) or after dilution with methanol. The compounds were separatedon reversed phase columns utilizing a gradient from 35 to 45 percentaqueous acetonitrile at flow rates ranging between 1 and 3 ml/min.Addition of glacial acetic acid or H₃ PO₄ (0.1 ml/L mobile phase) wasrequired for the separation of the free acids. Derivatives of7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3-(R),5(R)-dihydroxyheptanoicacid were detected by monitoring the absorbance at 238 nm, as well asthe absorbance ratio of 238 nm/228 nm. The desired products,6(R)-[2-[8(S)-(2-alkylacyloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one,were detected by monitoring the absorbance at 293 nm.

III.6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

Following the general procedure described above, the pH of the wholebroth from the bioconversion of twenty kilograms of the sodium salt of7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid (12,700 liters) was adjusted to 4.0 with 2N sulfuric acid and wasthen extracted with ethyl acetate (2×4500 l.). The whole brothextraction was followed by an extraction into 1N sodium bicarbonate (20%by volume) and the aqueous extract was then washed with ethyl acetate.To the aqueous extract was then added methylisobutylketone (MIBK, 570l.) and pH of the aqueous phase adjusted to 3.1 using 7.2N sulfuricacid. The MIBK extract of the acidified aqueous phase was then separatedfrom the aqueous phase which was then extracted with a second time MIBK(570 l.). The MIBK extracts are combined, filtered through diatomaceousearth, azeotropically dried and concentrated in vacuo to 870 liters. TheMIBK solution was heated to 95° C., and then treated withtrifluoroacetic acid (0.9 l.) in MIBK (23 l.). After about 15 minutes,the mixture was cooled to 25° C. and washed successively with 1N sodiumbicarbonate (0.5 volumes) and water (2×0.5 volumes). The organic phasewas concentrated in vacuo and the residue dissolved in acetonitrile,which was then diluted to 30% acetonitrile using 0.02M phosphate bufferat pH=7. Aliquots (1/3) which contain approximately 700 gm. of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-6-hydroxymethyl-2(S)-methyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-onewere chromatographed over an SP-207 (300 l, brominated copolymer ofstyrene and divinylbenzene, Mitsubishi Co.) column elution withacetonitrile/buffer (30%, 37%, 47%, 57%,) and acetonitrile/water (67%)gave the above titled product and the 6-hydroxymethyl compound as amixture. The desired product may be further purified by removing most ofthe 6-hydroxymethyl compound by crystallization by dissolving themixture in isopropyl, acetate (IPAC) or methyl-t-butyl ether (MTBE) andthen adding the solution to a non-polar solvent (n-heptane, cyclohexaneor petroleum ether).

IV. Isolation of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

The crystallization mother liquors from Step III were concentrated to anoil and then dissolved in toluene:methanol:acetonitrile (8:1:1, V:V:V)to a final volume of 100 ml. This solution was charged to a 10 litercolumn of Sephadex LH-20 (Pharmacia Inc.) equilibrated withhexane:toluene:methanol (3:1:1, V:V:V) and eluted with this solvent at aflow rate of 100 ml/min.

The desired compound eluted between 11 and 14 column volumes and therich cut eluant was concentrated to a solid. The product was furtherpurified by preparative reverse phase hplc on a C₁₈ column (21.4 mmID×30 cm) eluted with a linear gradient starting 10 minutes afterinjection from 25% acetonitrile in water to 75% acetonitrile in waterover 40 minutes at a flow rate of 10 ml/min. The fractions containingthe desired product (eluting at 29 minutes) were combined andconcentrated to yield about 400 mg. of the desired product incrystalline form. ¹³ C NMR Data (CD₂ Cl₂, δ_(c) =53.8 ppm)

    ______________________________________    ppm             ppm    ppm    ______________________________________    9.4             36.5   67.0    10.6            36.8   76.0    24.1            37.7   123.1    24.3            39.0   124.5    24.4            39.6   144.3    24.9            42.7   154.9    32.9            43.3   170.2    33.4            63.1   177.6                           203.4    ______________________________________

MS analysis showed a weak M⁺ ion at m/z 432 and fragment ions at m/z 316and 173 (base). UV spectrum exhibited a γ_(max) =290 nm, with ε=21,900.

In a similar fashion Nocardia autotrophica subsp. canberrica ATCC 35203(MA6181) was utilized in the bioconversion reaction with the sodium saltof7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2,2-dimethylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid to afford the desired products.

Additionally, the sodium salt of7-[1,2,6,7,8,8a(R)-hexahydro-2(S),6(R)-dimethyl-8(S)-(2-methylbutyryloxy)-1(S)-naphthyl]-3(R),5(R)-dihydroxyheptanoicacid, the sodium salt of ring opened lovastatin, was subjected toanalogous bioconversion reactions utilizing both N. autotrophic subsp.amethystina ATCC 35204 (MA6180) and N. autotrophic subsp. canberricaATCC 35203 (MA6181) to afford6(R)-[2-[8(S)-(2-methylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one.

EXAMPLE 2 Preparation of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,5,6,7,8,8a(R)-Octahydronaphthyl-1(S)]-ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

Thirty milligrams of the dienone product of example 1 (R₁=2-methyl-2-butyl, a=double bond), dissolved in 3 ml of ethyl acetate,was hydrogenated (1 atm H₂, room temperature) over 6 mg of 10% palladiumon carbon for 30 hours. Removal of the catalyst by filtration andevaporation of the solvent afforded the title compound. IR(film): 1718cm⁻¹, 1665 cm⁻¹. MS(EI): m/z 434 (M⁺).

EXAMPLE 3 Preparation of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one(a)6(R)-[2-[8(S)-(2,2-Dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(2')

Tert-Butyldimethylsilyl chloride (8 g, 52 mmol) was added to a stirredsolution of6(R)-[2-[8(S)-(2,2-Dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one(20 g, 48 mmol) and imidazole (6.8 g, 0.1 mol) in DMF (150 mL) at 0° C.The resulting mixture was stirred at 0° C. for 5 minutes, then warmed toroom temperature and stirred for 5 hours. TLC analysis of an aliquotindicated that the reaction was complete. The reaction mixture waspoured into cold water and extracted with ether. The ethereal extractwas washed with dilute hydrochloric acid, water and 5% sodiumbicarbonate solution. After drying over MgSO₄, the organic extract wasfiltered and the filtrate was concentrated in vacuo to afford thedesired product as a colorless, viscous oil: NMR (CDCl₃) δ 0.84 (3H, t,J=7 Hz), 0.89 (3H, d, J= 7 Hz), 0.90 (9H,s), 1.09 (3H, d, J=7 Hz), 1.11(3H, s), 1.12 (3H, s), 4.30 (H, m), 4.60 (H, m), 5.33 (H, m), 5.51 (H,m), 5.77 (H, d of d, J=10, 6 Hz), 5.98 (H, d, J=10 Hz).

(b)6(R)-[2-[5(S)-Chloro-4a(S)-hydroxy-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,4a,5,6,7,8,8a(S)-octahydronaphthyl-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(3')

A solution of phenylselenyl chloride (10 g, 52 mmol) in methylenechloride (50 mL) was added dropwise to a stirred solution of compound 2'(25.2 g, 48 mmol) in methylene chloride (350 mL) cooled in a dryice/i-propanol bath (-78° C.). The resulting mixture was stirred at -78°C. for 20 minutes, poured into cold water (300 mL) and extracted withether twice (400 mL, then 150 mL). The combined extracts were dried(MgSO₄), filtered and concentrated to afford an oily residue which wasdissolved in tetrahydrofuran (300 mL). This solution was chilled in anice bath (0° C.), and 30% hydrogen peroxide (15 mL) was added. Theresulting mixture was stirred at 0° C. for 5 minutes, then warmed toroom temperature and stirring continued for 1 hour. The reaction mixturewas poured into cold water and extracted with chloroform three times(400 mL, then 2× 100 mL). The combined extracts were dried (MgSO₄),filtered and concentrated to yield a residue which was purified by flashchromatography on a silica gel column. Elution with hexane:ethyl acetate(5:1/v:v) removed the impurities. Further elution with hexane:ethylacetate (4:1/v:v) provided the title compound as a pale yellow gum whichlater solidified on standing: mp 117°-8° C., NMR (CDCl₃) δ 0.075 (3H,s), 0.08 (3H, s), 0.85 (3H, t, J=7 Hz), 0.88 (9H, s), 0.89 (3H, d, J=7Hz), 1.15 (3H, s), 1.16 (3H, s), 1.32 (3H, d, J=7 Hz), 1.58 (2H, q, J=7Hz), 3.39 (H, s), 4.05 (H, br. s), 4.30 (H, m), 4.60 (H, m), 5.32 (H,m), 5.59 (H, d, J=11 Hz), 5.79 (H, d of d, J=11, 6 Hz).

Anal. Calcd. for C₃₁ H₅₃ C10₆ Si: C, 63.61; H, 9.13. Found: C, 63.80; H,9.04.

(c)6(R)-[2-[4a(S)-hydroxy-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,4a,5,6,7,8,8a(S)-octahydronaphthyl-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(4')

Tributyltin hydride (7.06 ml, 26.25 mmol) and azobisisobutyronitrile(AIBN) (0.82 g, 5.0 mmol) were added to a magnetically stirred solutionof chlorohydrin 3' (8.78 g, 15 mmol) in benzene (100 ml). The resultingsolution was refluxed for 2 hours, cooled and concentrated in vacuo to aviscous yellow oil which was stirred with pet ether (200 ml) at -15° C.(ice/acetone bath) to provide 4' as a fluffy, colorless solid (6.9 g, mp97°-9° C.). The filtrate was extracted with CH₃ CN (4×50 ml) to removeall of the product contained in the pet ether. The CH₃ CN extracts werecombined and concentrated to a colorless oil which was purified by flashchromatography on a silica gel column. Elution with ethyl acetone/hexane(1:3/v:v) gave a colorless solid (1.0 g) which was stirred in pet ether(25 ml) at 0° C. to remove some tin residues. The mixture was filteredto provide the product 4' as a colorless solid. M.P. 103°-4° C., nmr(CDCl₃) δ 0.07 (3H, s), 0.08 (3H, s), 0.88 (9H, s), 1.15 (3H, s), 1.16(3H, s), 1.20 (3H, d, J=7 Hz), 2.78 (H, s), 4.28 (H, m), 4.58 (H, m),5.30 (H, m), 5.58 (H, d, J=10 Hz), 5.67 (H, dd, J=10, 5 Hz).

Anal. Calcd. for C₃₁ H₅₄ O₆ Si: C, 67.59; H, 9.88. Found: C, 67.20; H,9.99.

(d)6(R)-[2-[3-oxo-8(S)-(2,2-dimethylbutyryloxy)-2(S)6-(R)-dimethyl-1,2,3,5,6,7,8,8a-octahydronaphthyl-1(S)]-ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one.(5')

7.2 g (12 mmol) of compound (4') was combined with 60 ml of toluene and42 g of pyridinum chlorochromate/aluminum oxide. The mixture was stirredand heated on a steam bath for 20 minutes after which time tlc showedthe reaction to be complete. The mixture was cooled, filtered and thesolids washed with warm toluene (4×50 ml). The solvent was evaporated toyield an amber gum. Nmr (CDCl₃) δ 0.073 (3H, s), 0.079 (3H, s), 0.804(3H, t, J=7 Hz), 0.881 (9H, s), 1.026 (2H, d, J=6 Hz), 1.036 (3H, d, J=6Hz), 1.10 (6H, br. s), 2.55-2.66 (3H, m), 4.276 (H, m), 4.588 (H, m)5.42 (H, m), 5.910 (H, d, J=1.5 Hz)

(e)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-3-(trimethylsilyloxy)-1,2,6,7,8,8a(R)-hexahydro-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one.(6')

The amber gum product of Step 3d was dissolved in methylene chloride andcooled to 0° C. under argon. The solution was treated with triethylamine(7.2 ml, 50 mmol) followed by slow addition of trimethylsilyltrifluoromethanesulfonate (5.4 ml, 28 mmol) while maintaining thetemperature below 3° C. After stirring at 0° C. for 15 minutes (tlcshowed the reaction to be complete by 5 minutes) the dark solution wasdiluted with methylene chloride (100 ml), washed with sat. NaHCO₃ (100ml), dried and the solvent evaporated.

(f)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one.(7')

The dark-amber residue of Step (2e) was dissolved inacetonitrile/tetrahydrofuran. Palladium (II) acetate (3.0 g, 13.0 mmol)was added to the mixture and the mixture stirred at room temperature for22 hours, at which time tlc showed the reaction to be complete. Themixture was filtered through a 3 cm pad, of silica gel and then washedwith ethyl acetate (150 ml), and the solvent evaporated. Nmr (CDCl₃) δ0.076 (3H, s) 0.082 (3H, s) 0.752 (3H, t, J=7 Hz) 0.883 (9H, s) 1.033(3H, d, J=7 Hz) 1.059 (3H, s) 1.065 (3H, s) 1.804 (3H, s) 4.295 (H, m)4.606 (H, m) 5.408 (H, m) 5.781 (H, br. s), 6.136 (H, br. s)

(g)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-furanone. (I)

The dark brown gum of Step (3f) was dissolved in tetrahydrofuran, and tothis was added a mixture of tetra-n-butyl ammonium fluoride (30 ml) andacetic acid (5.6 ml). The combined mixture was stirred at 50° C. for 4hours, cooled, diluted with ethyl ether (400 ml) washed with water(5×100 ml), dried and the solvent evaporated. The residue solidified toa brown mass. The brown mass was chromatographed on a 50 mm LP columnusing hexane-ethylacetate, 1:1 for the first 10 fractions (25 mlfractions) then 1:2 for 11, then 1:4. The titled product was found infractions 25-53, m.p. 160°-174° C. This chromatographed product was thenrecrystallized from ethyl acetate (30 ml)-hexane (30 ml). After dryingat 60° C. for 2 hours under a vacuum the titled product was obtainedwith M.P. 179°-180° C. Nmr (CDCl₃) δ 0.758 (3 H, t, J=7.4 Hz) 1.035 (3H,d, J=7.4 Hz) 1.063 (3H, s), 1.069 (3H, s), 1.867 (3H, s), 2.63 (H, ddd,J=1.47, 3.64, 12.6 Hz), 2.749 (H, dd, 4.94, 12,6 Hz) 4.398 (H, m), 4.645(H, m), 5.424 (H, m), 5.781 (H, br. s), 6.138 (H, br. s)

Anal. Calcd. for C₂₅ H₃₆ O₆ : C, 69.42; H, 8.39 Found: C, 69.73; H, 8.54

EXAMPLE 4 Preparation of6(R)-[2-[3-oxo-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,3,5,6,7,8,8a(R)-octahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-2,4,5,6-tetrahydro-2H-pyran-2-one.

A solution of compound (5') (500 mg, 0.9 mmol) of example 3 in aceticacid (42 ml) and water (15 ml) was heated at 70° C. for 3 hours. Aftercooling, the reaction mixture was diluted with water and extracted withether. The ethanol extract was washed with water five times, then washedwith aqueous sodium bicarbonate and brine. After drying and filtration,the filtrate was evaporated to afford a residue which was purified byflash chromatography on silica gel column. Elution of the column with30% of acetone in methylene chloride gave the title compound as a solid:mp 117°-8° C.; nmr (CDCl₃) δ 0.80 (3H, t, J=7 Hz), 1.02 (3H, d, J=7 Hz),1.04 (3H, d, J=7 Hz), 1.10 (6H, s), 2.64 (H, m of d, J=18 Hz), 2.72 (H,d of d, J=18, 4 Hz), 4.3H (H, m), 4.65 (H, m), 5.44 (H, m), 5.92 (H, br.s).

Anal. Calcd. for C₂₅ H₃₈ O₆ : C, 69.09; H, 8.81 Found: C, 68.85; H, 8.65

EXAMPLE 5 Preparation of6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one(a)6(R)-[2-[8(S)-(2,2-Dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]-ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(2')

Tert-Butyldimethylsilyl chloride (8 g, 52 mmol) was added to a stirredsolution of6(R)-[2-[8(S)-(2,2-Dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,6,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one(20 g, 48 mmol) and imidazole (6.8 g, 0.1 mol) in DMF (150 mL) at 0° C.The resulting mixture was stirred at 0° C. for 5 minutes, then warmed toroom temperature and stirred for 5 hours. TLC analysis of an aliquotindicated that the reaction was complete. The reaction mixture waspoured into cold water and extracted with ether. The ethereal extractwas washed with dilute hydrochloric acid, water and 5% sodiumbicarbonate solution. After drying over MgSO₄, the organic extract wasfiltered and the filtrate was concentrated in vacuo to afford thedesired product as a colorless, viscous oil: NMR (CDCl₃) δ 0.84 (3H, t,J=7 Hz), 0.89 (3H, d, J=7 Hz), 0.90 (9H, s), 1.09 (3H, d, J=7 Hz), 1.11(3H, s), 1.12 (3H, s), 4.30 (H, m), 4.60 (H, m), 5.33 (H, m), 5.51 (H,m), 5.77 (H, d of d, J=10, 6 Hz), 5.98 (H, d, J=10 Hz).

(b)6(R)-[2-[5(S)-Chloro-4a(S)-hydroxy-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-1,2,4a,5,6,7,8,8a(S)-octahydronaphthyl-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(3')

A solution of phenylselenyl chloride (10 g, 52 mmol) in methylenechloride (50 mL) was added dropwise to a stirred solution of compound 2'(25.2 g, 48 mmol) in methylene chloride (350 mL) cooled in a dryice/i-propanol bath (-78° C.). The resulting mixture was stirred at -78°C. for 20 minutes, poured into cold water (300 mL) and extracted withether twice (400 mL, then 150 mL). The combined extracts were dried(MgSO₄), filtered and concentrated to afford an oily residue which wasdissolved in tetrahydrofuran (300 mL). This solution was chilled in anice bath (0° C.), and 30% hydrogen peroxide (15 mL) was added. Theresulting mixture was stirred at 0° C. for 5 minutes, then warmed toroom temperature and stirring continued for 1 hour. The reaction mixturewas poured into cold water and extracted with chloroform three times(400 mL, then 2×100 mL). The combined extracts were dried (MgSO₄),filtered and concentrated to yield a residue which was purified by flashchromatography on a silica gel column. Elution with hexane:ethyl acetate(5:1/v:v) removed the impurities. Further elution with hexane:ethylacetate (4:1/v:v) provided the title compound as a pale yellow gum whichlater solidified on standing: mp 117°-8° C., NMR (CDCl₃) δ 0.075 (3H,s), 0.08 (3H, s), 0.85 (3H, t, J=7 Hz), 0.88 (9H, s), 0.89 (3H, d, J=7Hz), 1.15 (3H, s), 1.16 (3H, s), 1.32 (3H, d, J=7 Hz), 1.58 (2H, q, J=7Hz), 3.39 (H, s), 4.05 (H, br. s), 4.30 (H, m), 4.60 (H, m), 5.32 (H,m), 5.59 (H, d, J=11 Hz), 5.79 (H, d of d, J=11, 6 Hz).

Anal. Calcd. for C₃₁ H₅₃ ClO₆ Si: C, 63.61; H, 9.13. Found: C, 63.80; H,9.04.

(c)6(R)-[2-[5(S)-Chloro-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-3-oxo-1,2,3,5,6,7,8,8a(S)-octahydronaphthyl-1(S)]ethyl]-4(R)-(t-butyldimethylsilyloxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(13')

1.5 g (2.5 mmol) of compound (3') was combined with 20 ml of toluene and8 g of pyridinum chlorochromate/aluminum oxide. The mixture was stirredand heated at 110° C. for about 81/2 hours. The mixture was cooled,filtered, the solids washed with warm toluene (4×50 ml), and thefiltrates combined and evaporated to yield a light brown gum. NMR:(DCl₃), δ 0.069 (3H, s), 0.076 (3H, s), 0.804 (3H, t, J=7 Hz), 0.879(9H, s), 1.049 (3H, d, J=7 Hz), 1.094 (3H, s), 1.099 (3H, s), 1.135 (3H,d, J=7 Hz), 2.56-2.60 (H,m), 2.70 (H,m), 2.92 (H,m), 4.288 (H,m), 4.505(H, br. s), 4.584 (H,m), 5.43 (H,m), 6.06 (H, d, J 1 Hz)

(d)6(R)-[2-[5(S)-Chloro-8(S)-(2,2-dimethylbutyryloxy)-2(S),6(R)-dimethyl-3-oxo-1,2,3,5,6,7,8,8a(S)-octahydronaphthyl-2(S)]ethyl]-4(R)-(hydroxy)-3,4,5,6-tetrahydro-2H-pyran-2-one(14')

The light brown gum (13') was dissolved in acetonitrile (15 ml) underargon and cooled to 5° C. Aqueous hydrofluoric acid (45%), (750 μl) wasadded and the solution stirred at 20° C. for 11/2 hours (tlc showed thereaction to be complete after about 1 hour) and the mixture diluted withethyl ether (150 ml) and washed with saturated NaHCO₃ (3×25 ml), driedand the solvent evaporated.

(e)6(R)-[2-[8(S)-(2,2-dimethylbutyryloxy)-2(S),6-dimethyl-3-oxo-1,2,3,7,8,8a(R)-hexahydronaphthyl-1(S)]ethyl]-4(R)-hydroxy-3,4,5,6-tetrahydro-2H-pyran-2-one

To compound (14') from Step 5(d) dissolved in 2-butanone (20 ml) wasadded NaI (750 mg, 5 mmol) under argon and the mixture stirred at refluxfor 96 hours. The mixture was cooled, diluted with EtOAc (100 ml) andwashed with dilute Na₂ S₂ O₃ (100 ml), H₂ O (2×100 ml) and dried andevaporated. The residue was chromatographed on a 40 mm LP column usinghexane/EtOAc (25 ml fractions); 1:1 for 1-10 then 1:2 for 10-36, then1:4. The desired product was found in fractions 55-74 and wasrecrystallized from hexane:EtOAc (1:1) to yield tiny colorless needles,mp 174°-176° C.

NMR: (CDCl₃) δ 0.758 (3H, t, J=7.4 Hz) 1.035 (3H, d, J=7.4 Hz) 1.063(3H, s), 1.069 (3H, s), 1.867 (3H, s), 2.63 (H, ddd, J=1.47, 3.64, 12.6Hz), 2.749 (H, dd, 4.94, 12.6 Hz) 4.398 (H, m), 4.645 (H, m), 5.424 (H,m), 5.781 (H, br. s), 6.138 (H, br. s)

Anal. Calcd. for C₂₅ H₃₆ O₆ : C, 69.42; H, 8.39 Found: C, 69.73; H, 8.54

EXAMPLE 6-10

Following the procedure of Examples 3 and 5 and substituting anequivalent amount of reactant (A) for simvastatin in step (a), theproduct (B) is formed. ##STR20## Example 6 R₁ =2-butyl, R₂ =CH₃ ;

7 R₁ =2-butyl, R₂ =H;

8 R₁ =2-methyl-2-butyl, R₂ =H;

9 R₁ =2-methyl-2-butyl, R₂ =CH₂ OH;

10 (R₁ =2-butyl, R₂ =CH₂ OH.

EXAMPLE 11 Preparation of Ammonium Salts of Compounds II

The lactone (1.0 mmol) from Example 1 is dissolved with stirring in 0.1NNaOH (1.1 mmol) at ambient temperature. The resulting solution is cooledand acidified by the dropwise addition of 1N HCl. The resulting mixtureis extracted with diethyl ether and the extract washed with brine anddried (MgSO₄). The MgSO₄ is removed by filtration and the filtratesaturated with ammonia (gas) to give a gum which solidified to providethe ammonium salt.

EXAMPLE 12 Preparation of Alkali and Alkaline Earth Salts of CompoundsII

To a solution of 42 mg of lactone from Example 1 in 2 ml of ethanol isadded 1 ml of aqueous NaOH (1 equivalent). After one hour at roomtemperature, the mixture is taken to dryness in vacuo to yield thedesired sodium salt.

In like manner, the potassium salt is prepared using one equivalent ofpotassium hydroxide, and the calcium salt, using one equivalent of CaO.

EXAMPLE 13 Preparation of Ethylenediamine Salts of Compounds II

To a solution of 0.50 g of the ammonium salt from Example 11 in 10 ml ofmethanol is added 0.75 ml of ethylenediamine. The methanol is strippedoff under vacuum to obtain the desired ethylenediamine salt.

EXAMPLE 14 Preparation of Tris(hydroxymethyl)aminomethane Salts ofCompounds II

To a solution of 202 mg of the ammonium salt from Example 11 in 5 ml ofmethanol is added a solution of 60.5 mg oftris(hydroxymethyl)aminomethane in 5 ml of methanol. The solvent isremoved in vacuo to afford the desired tris(hydroxymethyl)aminomethanesalt.

EXAMPLE 15 Preparation of L-Lysine Salts of Compounds II

A solution of 0.001 mole of L-lysine and 0.0011 mole of the ammoniumsalt from Example 11 in 15 ml of 85% ethanol is concentrated to drynessin vacuo to give the desired L-lysine salt.

Similarly prepared are the L-arginine, L-ornithine, andN-methylglucamine salts.

EXAMPLE 16 Preparation of Tetramethylammonium Salts of Compounds II

A mixture of 68 mg of ammonium salt from Example 11 in 2 ml of methylenechloride and 0.08 ml of 24% tetramethylammonium hydroxide in methanol isdiluted with ether to yield the desired tetramethylammonium salt.

EXAMPLE 17 Preparation of Methyl Esters of Compounds II

To a solution of 400 mg of lactone from Example 1 in 100 ml of absolutemethanol is added 10 ml 0.1M sodium methoxide in absolute methanol. Thissolution is allowed to stand at room temperature for one hour, then isdiluted with water and extracted twice with ethyl acetate. The organicphase is separated, dried (Na₂ SO₄), filtered and evaporated in vacuo toyield the desired methyl ester.

In like manner, by the use of equivalent amounts of propanol, butanol,isobutanol, t-butanol, amylalcohol, isoamylalcohol,2-dimethylaminoethanol, benzylalcohol, 2-acetamidoethanol and the like,the corresponding esters are obtained.

EXAMPLE 18 Preparation of Free Dihydroxy Acids

The sodium salt of the compound II from Example 12 is dissolved in 2 mlof ethanol-water (1:1; v:v) and added to 10 ml of 1N hydrochloric acidfrom which the dihydroxy acid is extracted with ethyl acetate. Theorganic extract is washed once with water, dried (Na₂ SO₄), andevaporated in vacuo with a bath temperature not exceeding 30° C. Thedihydroxy acid derivative slowly reverts to the corresponding, parentlactone on standing, but is stable at a pH above 7.

EXAMPLE 19

As a specific embodiment of a composition of this invention, 20 mg oflactone from Example 1, is formulated with sufficient finely dividedlactose to provide a total amount of 580 to 590 mg to fill a size 0,hard-gelatin capsule.

What is claimed is:
 1. A compound of formula (III) ##STR21## wherein: R₁is selected from:(1) C₁₋₁₀ alkyl; (2) substituted C₁₋₁₀ alkyl in whichone or more substituent(s) is selected from(a) halogen, (b) hydroxy, (c)C₁₋₁₀ alkoxy, (d) C₁₋₅ alkoxycarbonyl, (e) C₁₋₅ acyloxy, (f) C₃₋₈cycloalkyl, (g) phenyl, (h) substituted phenyl in which the substituentsare X and Y, (i) C₁₋₁₀ alkylS(O)_(n) in which n is 0 to 2, (j) C₃₋₈cycloalkylS(O)_(n), (k) phenylS(O)_(n), (l) substituted phenylS(O)_(n)in which the substituents are X and Y, and (m) oxo; (3) C₁₋₁₀ alkoxy;(4) C₂₋₁₀ alkenyl; (5) C₃₋₈ cycloalkyl; (6) substituted C₃₋₈ cycloalkylin which one substituent is selected from(a) C₁₋₁₀ alkyl (b) substitutedC₁₋₁₀ alkyl in which one substituent is selected from(i) halogen, (ii)hydroxy, (iii) C₁₋₁₀ alkoxy, (iv) C₁₋₅ alkoxycarbonyl, (v) C₁₋₅ acyloxy,(vi) phenyl, (vii) substituted phenyl in which the substituents are Xand Y, (viii) C₁₋₁₀ alkylS(O)_(n) (ix) C₃₋₈ cycloalkylS(O)_(n), (x)phenylS(O)_(n), (xi) substituted phenylS(O)_(n) in which thesubstituents are X and Y, and (xii) oxo; (c) C₁₋₁₀ alkylS(O)_(n), (d)C₃₋₈ cycloalkylS(O)_(n), (e) phenylS(O)_(n), (f) substitutedphenylS(O)_(n) in which the substituents are X and Y, (g) halogen, (h)hydroxy, (i) C₁₋₁₀ alkoxy, (j) C₁₋₅ alkoxycarbonyl, (k) C₁₋₅ acyloxy,(l) phenyl, and (m) substituted phenyl in which the substituents are Xand Y; (7) phenyl; (8) substituted phenyl in which the substituents areX and Y; (9) amino; (10) C₁₋₅ alkylamino; (11) di(C₁₋₅ alkyl)amino; (12)phenylamino; (13) substituted phenylamino in which the substituents areX and Y; (14) phenyl C₁₋₁₀ alkylamino; (15) substituted phenyl C₁₋₁₀alkylamino in which the substituents are X and Y; (16) R₃ S in which R₃is selected from(a) C₁₋₁₀ alkyl, (b) phenyl, and (c) substituted phenylin which the substituents are X and Y; R₂ ' is H, CH₃, or CH₂ OT₃ ; T₁,T₂ and T₃ are each independently selected from: H, trimethylsilyl,triethylsilyl, tertbutyldimethylsilyl or tert-butyldiphenylsilyl,triisopropylsilyl; provided that where T₂ is H a and c are double bonds;and where T₂ is a silyl group b and d are double bonds provided that,where R₂ ' is H or CH₃ and R₁ is C₁₋₁₀ alkyl, T₂ is a silyl group.
 2. Acompound of claim 1 wherein:R₁ is selected from:(1) C₁₋₁₀ alkyl; (2)substituted C₁₋₁₀ alkyl in which one or more substituent(s) is selectedfrom(a) halogen, (b) hydroxy, (c) C₁₋₁₀ alkoxy, (d) C₁₋₅ alkoxycarbonyl,(e) C₁₋₅ acyloxy, (f) C₃₋₈ cycloalkyl, (g) phenyl, (h) substitutedphenyl in which the substituents are X and Y, and (i) oxo; (3) C₃₋₈cycloalkyl; (4) substituted C₃₋₈ cycloalkyl in which one substituent isselected from(a) C₁₋₁₀ alkyl, (b) substituted C₁₋₁₀ alkyl in which thesubstituent is selected from(i) halogen, (ii) hydroxy, (iii) C₁₋₁₀alkoxy (iv) C₁₋₅ acyloxy, (v) C₁₋₅ alkoxycarbonyl, (vi) phenyl, (vii)substituted phenyl in which the substituents are X and Y, and (viii)oxo, (c) halogen, (d) hydroxy, (e) C₁₋₁₀ alkoxy, (f) C₁₋₅alkoxycarbonyl, (g) C₁₋₅ acyloxy, (h) phenyl, (i) substituted phenyl inwhich the substituents are X and Y; (5) phenylamino; (6) substitutedphenylamino in which the substituents are X and Y; (7) phenylC₁₋₁₀alkylamino; and (8) substituted phenyl C₁₋₁₀ alkylamino in which thesubstituents are X and Y; X and Y are independently selected from:(a)OH, (b) F, (c) trifluoromethyl, (d) C₁₋₃ alkoxy, (e) hydrogen, (f) C₁₋₅alkyl.
 3. A compound of claim 2 wherein:R₁ is C₁₋₁₀ alkyl.
 4. A compoundof claim 3 wherein:R₁ is 2-butyl or 2-methyl-2-butyl; R'₂ is H or CH₃ ;T₁ is tert-butyldimethylsilyl or H.
 5. A compound of claim 4 selectedfrom the group wherein:a. R₁ is 2-methyl-2-butyl, R'₂ is CH₃, T₂ istrimethylsilyl and b and d are double bonds; b. R₁ is 2-methyl-2-butyl,R'₂ is CH₃, T₂ is H and a and c are double bonds.
 6. A compound offormula (IV) ##STR22## wherein: R₁ is selected from:(1) C₁₋₁₀ alkyl; (2)substituted C₁₋₁₀ alkyl in which one or more substituent(s) is selectedfrom(a) halogen, (b) hydroxy, (c) C₁₋₁₀ alkoxy, (d) C₁₋₅ alkoxycarbonyl,(e) C₁₋₅ acyloxy, (f) C₃₋₈ cycloalkyl, (g) phenyl, (h) substitutedphenyl in which the substituents are X and Y, (i) C₁₋₁₀ alkylS(O)_(n) inwhich n is 0 to 2, (j) C₃₋₈ cycloalklS(O)_(n), (k) phenylS(O)_(n), (l)substituted phenylS(O)_(n) in which the substituents are X and Y, and(m) oxo; (3) C₁₋₁₀ alkoxy; (4) C₂₋₁₀ alkenyl; (5) C₃₋₈ cycloalkyl; (6)substituted C₃₋₈ cycloakyl in which one substituent is selected from(a)C₁₋₁₀ alkyl (b) substituted C₁₋₁₀ alkyl in which the substituent isselected from(i) halogen, (ii) hydroxy, (iii) C₁₋₁₀ alkoxy, (iv) C₁₋₅alkoxycarbonyl, (v) C₁₋₅ acyloxy, (vi) phenyl, (vii) substituted phenylin which the substituents are X and Y (viii) C₁₋₁₀ alkylS(O)_(n), (ix)C₃₋₈ cycloalkylS(O)_(n), (x) phenylS(O)_(n), (xi) substitutedphenylS(O)_(n) in which the substituents are X and Y, and (xii) oxo, (c)C₁₋₁₀ alkylS(O)_(n), (d) C₃₋₈ cycloalkylS(O)_(n), (e) phenylS(O)_(n),(f) substituted phenylS(O)_(n) in which the substituents are X and Y,(g) halogen, (h) hydroxy, (i) C₁₋₁₀ alkoxy, (j) C₁₋₅ alkoxycarbonyl, (k)C₁₋₅ acyloxy, (l) phenyl, and (m) substituted phenyl in which thesubstituents are X and Y; (7) phenyl; (8) substituted phenyl in whichthe substituents are X and Y; (9) amino; (10) C₁₋₅ alkylamino; (11)di(C₁₋₅ alkyl)amino; (12) phenylamino; (13) substituted phenylamino inwhich the substituents are X and Y; (14) phenyl C₁₋₁₀ alkylamino; (15)substituted phenyl C₁₋₁₀ alkylamino in which the substituents are X andY; (16) R₃ S in which R₃ is selected from(a) C₁₋₁₀ alkyl, (b) phenyl,and (c) substituted phenyl in which the substituents are X and Y; R'₂ isH, CH₃, or CH₂ OT; T₁ is selected from:H, trimethylsilyl, triethylsilyl,tert-butyldimethylsilyl or tert-butyldiphenylsilyl, ortriisopropylsilyl; W is Cl or Br; X and Y are selected from:(a) OH, (b)halogen, (c) trifluoromethyl, (d) C₁₋₃ alkoxy, (e) C₁₋₃alkylcarbonyloxy, (f) phenylcarbonyloxy, (g) C₁₋₃ alkoxycarbonyl, (h)phenyloxycarbonyl, (i) hydrogen; (j) C₁₋₅ alkyl; halogen is Cl or F. 7.A compound of claim 6 wherein:R₁ is selected from:(1) C₁₋₁₀ alkyl; (2)substituted C₁₋₁₀ alkyl in which one or more substituent(s) is selectedfrom(a) halogen, (b) hydroxy, (c) C₁₋₁₀ alkoxy, (d) C₁₋₅ alkoxycarbonyl,(e) C₁₋₅ acyloxy, (f) C₃₋₈ cycloalkyl, (g) phenyl, (h) substitutedphenyl in which the substituents are X and Y, and (i) oxo; (3) C₃₋₈cycloalkyl; (4) substituted C₃₋₈ cycloalkyl in which one substituent isselected from(a) C₁₋₁₀ alkyl, (b) substituted C₁₋₁₀ alkyl in which thesubstituent is selected from(i) halogen, (ii) hydroxy, (iii) C₁₋₁₀alkoxy (iv) C₁₋₅ acyloxy, (v) C₁₋₅ alkoxycarbonyl, (vi) phenyl, (vii)substituted phenyl in which the substituents are X and Y, and (viii)oxo, (c) halogen, (d) hydroxy, (e) C₁₋₁₀ alkoxy, (f) C₁₋₅alkoxycarbonyl, (g) C₁₋₅ acyloxy, (h) phenyl, (i) substituted phenyl inwhich the substituents are X and Y; (5) phenylamino; (6) substitutedphenylamino in which the substituents are X and Y; (7) phenylC₁₋₁₀alkylamino; and (8) substituted phenyl C₁₋₁₀ alkylamino in which thesubstituents are X and Y; X and Y are independently selected from:(a)OH, (b) F, (c) trifluoromethyl, (d) C₁₋₃ alkoxy, (e) hydrogen, (f) C₁₋₅alkyl.
 8. A compound of claim 7 wherein:R₁ is C₁₋₁₀ alkyl.
 9. A compoundof claim 8 wherein:R₁ is 2-butyl or 2-methyl-2-butyl; R'₂ is H or CH₃ ;T₁ is tert-butyldimethylsilyl or H.
 10. A compound of claim 9 selectedfrom the group wherein:a. R₁ is 2-methyl-2-butyl, R'₂ is CH₃, T₁ is H, Wis Cl; b. R₁ is 2-methyl-2-butyl, R'₂ is CH₃, T₁ istert-butyldimethylsilyl, W is Cl.